Super-resolution microscopes showcase the inner lives of cells
Using a tiny, spherical glass lens sandwiched between two brass plates, the 17th-century Dutch microscopist was the first to officially describe red blood cells and sperm cells in human tissues, and observe 鈥 in the water of a lake.
followed, revealing cell organelles like the nucleus and energy-producing mitochondria. But by 1873, scientists realized there was a limit to the level of detail. When light passes through a lens, the light gets spread out through diffraction. This means that two objects can鈥檛 be distinguished if they鈥檙e less than roughly 250 nanometers (250 billionths of a meter) apart 鈥 instead, they鈥檒l appear as a blur. That put the inner workings of cell structures off limits.
Electron microscopy, which uses electron beams instead of light, offers higher resolution. But the resulting black-and-white images make it hard tell proteins apart, and the method only works on dead cells.
Now, however, optics engineers and physicists have developed sophisticated tricks to overcome the diffraction limit of light microscopes, opening up a new world of detail. These techniques can distinguish objects down to 100 nanometers and sometimes even less than 10 nanometers. Scientists attach tiny, colored fluorescent tags to individual proteins or bits of DNA, often in living cells, where they can watch them in action. As a result, they are now filling in key knowledge gaps about how cells work and what goes wrong in neurological diseases and cancers, or during viral infections.
鈥淲e can really see new biology 鈥 things that we were hoping to see but hadn鈥檛 seen before,鈥 says molecular cell biologist , who directs an imaging center at the University of Oxford in the United Kingdom. highlights some of what scientists are learning in this new age of light microscopy.
Overcoming the diffraction limit
Super-resolution microscopy uses a variety of techniques to detect detail that would normally be hidden by the diffraction limit, Schermelleh explains. Single-molecule localization microscopy, for instance, takes advantage of the fact that spots on an image are easier to localize with precision when they appear in isolation rather than clustered together. Scientists label the molecules of interest with fluorescent tags designed to spontaneously emit light. As the probes twinkle on and off, computational models estimate exactly where each molecule is located 鈥 and reconstruct a high-resolution image of the sample.
Another technique, stimulated emission depletion, scans the samples with lasers that are surrounded by a second, donut-shaped ring of lasers that cancel out the fluorescent light around the area of interest, sharpening the microscope鈥檚 resolution. A third method, called structured illumination microscopy, illuminates samples with a striped pattern of light. These stripes interfere with the light emanating from the sample in ways that allow scientists to infer additional detail about the image.
The fundamentals of these techniques were developed in the early 2000s, but they鈥檝e only recently become widespread and accessible enough for biologists to use routinely, Schermelleh says. 鈥淲e now have really lots of projects that use super-resolution microscopy as a genuine tool for biological discovery,鈥 he says, 鈥渘ot just for making nice images.鈥
Revising biology textbooks
These techniques have already revealed new cell structures. Scientists have discovered that neurons have a unique kind of scaffold, called the , or MPS, which provides rigidity and form and that pass from one neuron to the next and to maintain the cells鈥 overall function. 鈥淭he MPS is involved in almost all the neuronal functions,鈥 says Columbia University neurobiologist Victor Macarr贸n-Palacios, who recently reported with colleagues that a particular protein, paralemmin-1, is responsible for .
Other cell structures, too, turn out to be more complex than they seemed. Earlier in 2025, biophysicist of the University of Pennsylvania and colleagues discovered that organelles called lysosomes, whose textbook role is to break down waste material in cells, can on their surfaces. This likely relates to additional functions that specific lysosomes have, such as sensing nutrients and repairing broken membranes.
Scientists also have been studying how organelles interact with one another. Cell biologist of the Howard Hughes Medical Institute鈥檚 Janelia Research Campus in Virginia, for instance, is scrutinizing the structures that use to dock onto the protein-making endoplasmic reticulum, which supplies calcium and fats to mitochondria.
Such studies might help reveal the causes of disease. Last year, Lippincott-Schwartz learned that , which is believed to contribute to the (ALS), may interfere with the ability of the endoplasmic reticulum to connect to mitochondria, she says. This could alter the function of these powerhouses and help explain . 鈥淲e鈥檙e just learning what these various genetic mutations that underlie some of these diseases are actually doing at the cell biological level.鈥
Gazing into human DNA
Scientists have also been peering into the nucleus and studying the DNA inside it. Human DNA, if removed from a single cell and stretched out, would span about 2 yards. To squeeze inside the nucleus, it wraps itself around , creating a string-of-beads combo known as chromatin. The chromatin further loops and twists to form our chromosomes.
Chromatin loops and bunches, or domains, can only be studied in detail with super-resolution microscopy, for instance by tagging segments of DNA with fluorescent probes, says Schermelleh, who has been studying how the in mammalian cells. 鈥淭he size scale is just below the diffraction limit, so it couldn鈥檛 be assessed before.鈥
Research by Lakadamyali has revealed, for instance, that the DNA-histone strings of beads organize into than scientists had assumed, with some regions of DNA more tightly packed than others.
This packaging determines how accessible a given region of DNA is. And that鈥檚 important because different cells in the body, say heart cells or neurons, use only a specific subset of their genes. The ones they use are left in a looser, more accessible state, while the silenced ones are packed tight.
In 2015, Lakadamyali found that embryonic stem cells, which can develop into any cell type, compared to more specialized cells, which have silenced the genes they don鈥檛 need. 鈥淲e can actually determine whether a cell is a stem cell or a differentiated cell based on the spatial organization of chromatin,鈥 says Lakadamyali, who coauthored a 2023 in the Annual Review of Biophysics.
Improving cancer therapies
Scientists are also examining cells affected by disease. For example, biophysicist of the University of W眉rzburg in Germany is studying certain receptor proteins on the surfaces of cancer cells that are used as targets in cancer-killing therapies. For blood cancers, for instance, scientists have genetically engineered immune cells to find and kill cancer cells that have specific surface proteins.
But the techniques commonly used to analyze the proteins in patients鈥 cancer cells and match patients with effective therapies don鈥檛 give a full picture, Sauer says. That was illustrated back in 2015, when physicians discovered they could successfully treat patients with the blood cancer multiple myeloma with 鈥 even though CD19 hadn鈥檛 been spotted on multiple myeloma cancer cells with standard methods.
Sauer and colleagues found in 2019 that the with super-resolution microscopy. They learned that to do their killing job, the immune therapies require as few as 10 CD19 proteins among hundreds or thousands of other proteins on a cancer cell surface.
These microscopy techniques can be used to better match patients to effective therapies, Sauer says. His more recent research has for therapies to target, and helped 鈥 knowledge that could help improve the potency of immune therapies. 鈥淵ou have to visualize those processes at molecular level,鈥 he says.
Filming viral invasions
The wily tricks viruses use to infect human cells and reproduce are also under investigation. Understanding such dynamics could help scientists develop new antiviral medicines, says virologist of the Helmholtz Centre for Infection Research in Germany.
Earlier in 2025, for example, Sieben reported how the infects human cells. By tagging viral and human proteins, he and colleagues watched the virus first latch onto single receptor proteins on the cell surface. The virus then waited until other receptor proteins, moving around in the fluid cell membrane, accumulated nearby. Only could it enter the cell, Sieben and his colleagues learned.
And in 2024, a team of scientists at Stanford University examined how the replicates inside human cells. Using fluorescent tags to label the virus鈥檚 genetic material, biophysicist and colleagues found that with a double membrane in which it copies its genetic material. This probably prevents destruction by the cell, Andronov says.
As more and more scientists use super-resolution microscopy to illuminate the goings-on inside cells, how much more detail can they expect to see? Refinements like creating smaller fluorescent probes 鈥 so that one can label multiple sites along a single protein 鈥 could push the resolution further, Lakadamyali says.
Perhaps one day super-resolution advances might rival those of electron microscopy. After all, just two decades ago, 鈥渨e didn鈥檛 know that we could break the diffraction limit,鈥 she says. 鈥淲e鈥檝e made so much progress in a 20-year period. I think it鈥檚 possible.鈥
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